FDA recall Z-2365-2018
Zimmer Biomet, Inc. · Class II · device
Product
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00
Reason for recall
—
Distribution
Products were distributed solely to Japan.
Key facts
- Status
- Terminated
- Initiation date
- 2018-05-30
- Report date
- 2018-07-11
- Termination date
- 2020-05-28
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Warsaw, IN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2365-2018